Packages / Debian 13 (Trixie) / metapackages / med-cloud
Package: med-cloud (3.9.0)
Maintainers:
Similar packages:
- [med-all]
Default selection of tasks for Debian Med
- [med-bio]
Debian Med bioinformatics packages
- [med-bio-dev]
Debian Med packages for development of bioinformatics applications
- [med-config]
Debian Med general config package
- [med-data]
Debian Med drug databases
- [med-dental]
Debian Med packages related to dental practice
- [med-epi]
Debian Med epidemiology related packages
- [med-his]
Debian Med suggestions for Hospital Information Systems
- [med-imaging]
Debian Med image processing and visualization packages
- [med-imaging-dev]
Debian Med image processing and visualization packages development
- [med-laboratory]
Debian Med suggestions for medical laboratories
- [med-oncology]
Debian Med packages for oncology
- [med-pharmacy]
Debian Med packages for pharmaceutical research
- [med-physics]
Debian Med packages for medical physicists
- [med-practice]
Debian Med packages for practice management
- [med-psychology]
Debian Med packages for psychology
- [med-research]
Debian Med packages for medical research
- [med-statistics]
Debian Med statistics
- [med-tasks]
Debian Med tasks for tasksel
- [med-tools]
Debian Med several tools
- [med-typesetting]
Debian Med support for typesetting and publishing
Debian Med bioinformatics applications usable in cloud computing
Other Packages Related to med-cloud:
dep: [med-config] (= 3.9.0)
Debian Med general config package
dep: [med-tasks] (= 3.9.0)
Debian Med tasks for tasksel
rec: [abyss]
de novo, parallel, sequence assembler for short reads
rec: [aevol]
digital genetics model to run Evolution Experiments in silico
rec: [alien-hunter]
Interpolated Variable Order Motifs to identify horizontally acquired DNA
rec: [altree]
program to perform phylogeny-based association and localization analysis
rec: [amap-align]
Protein multiple alignment by sequence annealing
rec: [ampliconnoise]
removal of noise from 454 sequenced PCR amplicons
rec: [aragorn]
tRNA and tmRNA detection in nucleotide sequences
rec: [arden]
specificity control for read alignments using an artificial reference
rec: [autodock]
analysis of ligand binding to protein structure
rec: [autodock-vina]
docking of small molecules to proteins
rec: [autogrid]
pre-calculate binding of ligands to their receptor
rec: [bamtools]
toolkit for manipulating BAM (genome alignment) files
rec: [bedtools]
suite of utilities for comparing genomic features
rec: [bioperl]
Perl tools for computational molecular biology
rec: [bioperl-run]
BioPerl wrappers: scripts
rec: [biosquid]
utilities for biological sequence analysis
rec: [bowtie]
Ultrafast memory-efficient short read aligner
rec: [bowtie2]
ultrafast memory-efficient short read aligner
rec: [boxshade]
Pretty-printing of multiple sequence alignments
rec: [bwa]
Burrows-Wheeler Aligner
rec: [cassiopee]
index and search tool in genomic sequences
rec: [cd-hit]
suite of programs designed to quickly group sequences
rec: [cdbfasta]
Constant DataBase indexing and retrieval tools for multi-FASTA files
rec: [circos]
plotter for visualizing data
rec: [clearcut]
extremely efficient phylogenetic tree reconstruction
rec: [clonalframe]
inference of bacterial microevolution using multilocus sequence data
rec: [clustalo]
General-purpose multiple sequence alignment program for proteins
rec: [clustalw]
global multiple nucleotide or peptide sequence alignment
rec: [concavity]
predictor of protein ligand binding sites from structure and conservation
rec: [conservation-code]
protein sequence conservation scoring tool
rec: [datamash]
statistics tool for command-line interface
rec: [dialign]
Segment-based multiple sequence alignment
rec: [dialign-tx]
Segment-based multiple sequence alignment
rec: [discosnp]
discovering Single Nucleotide Polymorphism from raw set(s) of reads
rec: [disulfinder]
cysteines disulfide bonding state and connectivity predictor
rec: [dnaclust]
tool for clustering millions of short DNA sequences
rec: [dssp]
protein secondary structure assignment based on 3D structure
rec: [embassy-domainatrix]
Extra EMBOSS commands to handle domain classification file
rec: [embassy-domalign]
Extra EMBOSS commands for protein domain alignment
rec: [embassy-domsearch]
Extra EMBOSS commands to search for protein domains
rec: [emboss]
European molecular biology open software suite
rec: [exonerate]
generic tool for pairwise sequence comparison
rec: [fastdnaml]
Tool for construction of phylogenetic trees of DNA sequences
rec: [fastlink]
faster version of pedigree programs of Linkage
rec: [fastqc]
quality control for high throughput sequence data
rec: [fasttree]
phylogenetic trees from alignments of nucleotide or protein sequences
rec: [fitgcp]
fitting genome coverage distributions with mixture models
rec: [flexbar]
flexible barcode and adapter removal for sequencing platforms
rec: [freecontact]
fast protein contact predictor
rec: [gasic]
genome abundance similarity correction
rec: [genometools]
versatile genome analysis toolkit
rec: [gff2aplot]
pair-wise alignment-plots for genomic sequences in PostScript
rec: [gff2ps]
produces PostScript graphical output from GFF-files
rec: [glam2]
gapped protein motifs from unaligned sequences
rec: [gmap]
spliced and SNP-tolerant alignment for mRNA and short reads
rec: [grinder]
Versatile omics shotgun and amplicon sequencing read simulator
rec: [gromacs]
Molecular dynamics simulator, with building and analysis tools
rec: [hhsuite]
sensitive protein sequence searching based on HMM-HMM alignment
rec: [hisat2]
graph-based alignment of short nucleotide reads to many genomes
rec: [hmmer]
profile hidden Markov models for protein sequence analysis
rec: [idba]
iterative De Bruijn Graph short read assemblers
rec: [infernal]
inference of RNA secondary structural alignments
rec: [jellyfish]
count k-mers in DNA sequences
rec: [kalign]
Global and progressive multiple sequence alignment
rec: [kissplice]
Detection of various kinds of polymorphisms in RNA-seq data
rec: [last-align]
genome-scale comparison of biological sequences
rec: [loki]
MCMC linkage analysis on general pedigrees
rec: [macs]
Model-based Analysis of ChIP-Seq on short reads sequencers
rec: [mafft]
Multiple alignment program for amino acid or nucleotide sequences
rec: [mapsembler2]
bioinformatics targeted assembly software
rec: [maq]
maps short fixed-length polymorphic DNA sequence reads to reference sequences
rec: [melting]
compute the melting temperature of nucleic acid duplex
rec: [minia]
short-read biological sequence assembler
rec: [mipe]
Tools to store PCR-derived data
rec: [mira-assembler]
Whole Genome Shotgun and EST Sequence Assembler
rec: [mlv-smile]
Find statistically significant patterns in sequences
rec: [mothur]
sequence analysis suite for research on microbiota
rec: [mrbayes]
Bayesian Inference of Phylogeny
rec: [mummer]
Efficient sequence alignment of full genomes
rec: [muscle]
Multiple alignment program of protein sequences
rec: [muscle3]
multiple alignment program of protein sequences
rec: [mustang]
multiple structural alignment of proteins
rec: [ncbi-epcr]
Tool to test a DNA sequence for the presence of sequence tagged sites
rec: [ncbi-tools-bin]
NCBI libraries for biology applications (text-based utilities)
rec: [ncoils]
coiled coil secondary structure prediction
rec: [neobio]
computes alignments of amino acid and nucleotide sequences
rec: [paraclu]
Parametric clustering of genomic and transcriptomic features
rec: [parsinsert]
Parsimonious Insertion of unclassified sequences into phylogenetic trees
rec: [pdb2pqr]
Preparation of protein structures for electrostatics calculations
rec: [perm]
efficient mapping of short reads with periodic spaced seeds
rec: [phyml]
Phylogenetic estimation using Maximum Likelihood
rec: [phyutility]
simple analyses or modifications on both phylogenetic trees and data matrices
rec: [picard-tools]
Command line tools to manipulate SAM and BAM files
rec: [plink]
whole-genome association analysis toolset
rec: [plink1.9]
whole-genome association analysis toolset
rec: [plink2]
whole-genome association analysis toolset
rec: [poa]
Partial Order Alignment for multiple sequence alignment
rec: [prank]
Probabilistic Alignment Kit for DNA, codon and amino-acid sequences
rec: [prime-phylo]
bayesian estimation of gene trees taking the species tree into account
rec: [primer3]
tool to design flanking oligo nucleotides for DNA amplification
rec: [probabel]
Toolset for Genome-Wide Association Analysis
rec: [probcons]
PROBabilistic CONSistency-based multiple sequence alignment
rec: [proda]
multiple alignment of protein sequences
rec: [prodigal]
Microbial (bacterial and archaeal) gene finding program
rec: [python3-biomaj3-cli]
BioMAJ client
rec: [python3-biopython]
Python3 library for bioinformatics
rec: [r-bioc-edger]
Empirical analysis of digital gene expression data in R
rec: [r-bioc-hilbertvis]
GNU R package to visualise long vector data
rec: [r-cran-pvclust]
Hierarchical Clustering with P-Values via Multiscale Bootstrap
rec: [r-cran-qtl]
GNU R package for genetic marker linkage analysis
rec: [r-cran-vegan]
Community Ecology Package for R
rec: [r-other-mott-happy.hbrem]
GNU R package for fine-mapping complex diseases
rec: [raster3d]
tools for generating images of proteins or other molecules
rec: [readseq]
Conversion between sequence formats
rec: [rnahybrid]
Fast and effective prediction of microRNA/target duplexes
rec: [rtax]
Classification of sequence reads of 16S ribosomal RNA gene
rec: [samtools]
processing sequence alignments in SAM, BAM and CRAM formats
rec: [seqan-apps]
C++ library for the analysis of biological sequences
rec: [sibsim4]
align expressed RNA sequences on a DNA template
rec: [sigma-align]
Simple greedy multiple alignment of non-coding DNA sequences
rec: [sim4]
tool for aligning cDNA and genomic DNA
rec: [smalt]
Sequence Mapping and Alignment Tool
rec: [snap]
location of genes from DNA sequence with hidden markov model
rec: [soapdenovo]
short-read assembly method to build de novo draft assembly
rec: [soapdenovo2]
short-read assembly method to build de novo draft assembly
rec: [sra-toolkit]
utilities for the NCBI Sequence Read Archive
rec: [ssake]
genomics application for assembling millions of very short DNA sequences
rec: [staden-io-lib-utils]
programs for manipulating DNA sequencing files
rec: [t-coffee]
Multiple Sequence Alignment
rec: [tabix]
generic indexer for TAB-delimited genome position files
rec: [theseus]
superimpose macromolecules using maximum likelihood
rec: [tigr-glimmer]
Gene detection in archea and bacteria
rec: [tree-puzzle]
Reconstruction of phylogenetic trees by maximum likelihood
rec: [tree-ppuzzle]
Parallelized reconstruction of phylogenetic trees by maximum likelihood
rec: [vcftools]
Collection of tools to work with VCF files
rec: [velvet]
Nucleic acid sequence assembler for very short reads
rec: [veryfasttree]
Speeding up the estimation of phylogenetic trees from sequences
rec: [wise]
comparison of biopolymers, like DNA and protein sequences
sug: acedb-other
Package not available
sug: anfo
Package not available
sug: bagpipe
Package not available
sug: blast2
Package not available
sug: [cufflinks]
Transcript assembly, differential expression and regulation for RNA-Seq
sug: embassy-phylip
Package not available
sug: giira
Package not available
sug: python3-cogent3
Package not available
sug: qiime
Package not available
Download med-cloud
| Architecture | Package Size | Installed Size | Files |
|---|---|---|---|
| all | 9.8 KiB | 30 KiB | [list of files] |
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Field source: Debian 13 (Trixie) main amd64 revision trixie-main-amd64:3ab4e811cf4f3e5a335d382c58cc19d85f1abe7a4ef4689160ca1f637fa0e9b3
